Product image of Lacosamide Accord (Lacosamide) supplied by GNH India

Lacosamide Accord

Active Ingredient:
Lacosamide
Origin:
EU

Lacosamide Accord (Lacosamide)

Lacosamide, the active ingredient in Lacosamide Accord, is a sodium channel blocker presented as an oral tablet for oral use. It is indicated for the adjunctive treatment of partial‑onset seizures in patients with epilepsy. It is formulated for systemic absorption and is marketed across the European Union.

GNH India supplies Lacosamide Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory documentation for import and distribution.

Manufacturer / TM Owner

Accord Healthcare S.L.U.

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Indications & Clinical Uses

Lacosamide is used in the management of epilepsy, specifically targeting focal seizure activity.

  • Partial‑onset seizures: Reduces seizure frequency when added to existing antiepileptic therapy.
  • Focal epilepsy: Improves seizure control as adjunctive treatment in patients with refractory focal seizures.
  • Adjunctive therapy for refractory seizures: Provides additional seizure reduction in individuals not adequately controlled by other medications.

How It Works

  • Lacosamide enhances the slow inactivation of voltage‑gated sodium channels in neuronal membranes, stabilizing hyper‑excitable neuronal membranes and decreasing repetitive neuronal firing. By selectively targeting the persistent sodium current, it reduces neuronal hyperexcitability without affecting normal rapid channel activity, contributing to seizure control. The drug does not significantly alter cardiac conduction at therapeutic doses, and its effect is additive to other antiepileptic agents.

Side Effects

Lacosamide may cause a range of adverse reactions, varying from mild to serious.

Common Side Effects

  • Dizziness
  • Nausea
  • Fatigue
  • Headache
  • Diplopia
  • Blurred vision

Serious or Rare Side Effects

  • Cardiac arrhythmias (e.g., atrial fibrillation, PR interval prolongation)
  • Suicidal thoughts or behavior
  • Severe skin reactions (e.g., Stevens‑Johnson syndrome)
  • Hypersensitivity reactions (e.g., angioedema, anaphylaxis)
  • Rhabdomyolysis
  • Hepatic enzyme elevations

Precautions & Warnings

When prescribing lacosamide, clinicians should consider several safety precautions to minimize risk.

  • Cardiac assessment: Obtain baseline ECG to evaluate PR interval and cardiac conduction.
  • Suicidality monitoring: Observe patients for signs of depression or suicidal ideation during therapy.
  • Renal impairment: Adjust dose in patients with moderate to severe renal dysfunction.
  • Hepatic impairment: Use caution and consider dose reduction in patients with liver disease.
  • Discontinuation: Do not stop abruptly; taper the dose to avoid seizure exacerbation.
  • Store at room temperature: Keep in the original container, protect from moisture and excessive heat.

Avoid Interactions

Lacosamide can interact with other medicines that affect its metabolism or cardiac conduction.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): May increase lacosamide plasma concentrations.
  • Concomitant drugs that prolong PR interval (e.g., beta‑blockers, digoxin): May enhance cardiac conduction effects.
  • Monoamine oxidase inhibitors: Potential for additive CNS effects.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., carbamazepine, phenytoin, rifampin): May reduce lacosamide levels.
  • Alcohol: May increase central nervous system depression.
  • Other antiepileptic drugs: May require dose adjustments to maintain efficacy.

Frequently Asked Questions

Lacosamide Accord is prescribed as an adjunctive treatment for partial‑onset (focal) seizures in patients with epilepsy. It is added to existing antiepileptic regimens when seizure control remains insufficient, helping to reduce the frequency of breakthrough seizures.

Lacosamide enhances the slow inactivation of voltage‑gated sodium channels in neurons. This stabilizes hyper‑excitable membranes, reduces repetitive firing, and limits the spread of epileptic activity without markedly affecting normal rapid sodium channel function.

The dose of Lacosamide Accord is individualized by the prescribing clinician based on the patient’s age, renal function, and response to therapy. The prescriber determines the appropriate starting dose and titration schedule according to clinical guidelines.

The safety of lacosamide in pregnancy and lactation has not been definitively established. Healthcare providers should weigh potential benefits against unknown risks and discuss alternative options with pregnant or nursing patients.

To request Lacosamide Accord, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Compared with older sodium‑channel blockers such as carbamazepine or phenytoin, lacosamide selectively enhances slow inactivation, which may result in fewer drug‑interaction concerns and a different side‑effect profile. It is often chosen when patients need additional seizure control without the enzyme‑inducing properties of some alternatives.

Lacosamide Accord should be stored at room temperature, below 25 °C, in its original packaging. Protect the product from moisture, direct sunlight and excessive heat to maintain potency throughout its shelf life.

The medication is taken orally. Patients should swallow the tablet whole with water and may take it with or without food, following the prescriber’s instructions regarding timing and any dose‑adjustments.

Serious risks include cardiac arrhythmias such as atrial fibrillation or PR‑interval prolongation, suicidal thoughts or behaviors, severe skin reactions like Stevens‑Johnson syndrome, hypersensitivity reactions (e.g., anaphylaxis), and rare cases of rhabdomyolysis. Prompt medical attention is required if any of these occur.

Lacosamide Accord is contraindicated in individuals with known hypersensitivity to lacosamide or any of its excipients, and in patients with severe cardiac conduction disorders (e.g., second‑ or third‑degree AV block) unless a pacemaker is in place. Caution is also advised for those with significant renal or hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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